Complexes of Sendai virus NP-P and P-L proteins are required for defective interfering particle genome replication in vitro.
about
Paramyxovirus RNA synthesis and the requirement for hexamer genome length: the rule of six revisitedInitiation and regulation of paramyxovirus transcription and replicationTrafficking of Sendai virus nucleocapsids is mediated by intracellular vesiclesCrystal structure of the Lassa virus nucleoprotein-RNA complex reveals a gating mechanism for RNA bindingRecombinant influenza virus polymerase: requirement of both 5' and 3' viral ends for endonuclease activity.Identification of temperature-sensitive mutations in the phosphoprotein of respiratory syncytial virus that are likely involved in its interaction with the nucleoprotein.Sendai virus C proteins must interact directly with cellular components to interfere with interferon actionComparison of the transcription and replication strategies of marburg virus and Ebola virus by using artificial replication systemsMapping the interacting domains between the rabies virus polymerase and phosphoprotein.A role for the Sendai virus P protein trimer in RNA synthesis.Three of the four nucleocapsid proteins of Marburg virus, NP, VP35, and L, are sufficient to mediate replication and transcription of Marburg virus-specific monocistronic minigenomes.Mutations in the 5' trailer region of a respiratory syncytial virus minigenome which limit RNA replication to one step.Peste des petits ruminants virus infection of small ruminants: a comprehensive review.Nucleocapsid incorporation into parainfluenza virus is regulated by specific interaction with matrix protein.Surface expression of the hRSV nucleoprotein impairs immunological synapse formation with T cells.Activity of polymerase proteins of vaccine and wild-type measles virus strains in a minigenome replication assay.Chemical modification of nucleotide bases and mRNA editing depend on hexamer or nucleoprotein phase in Sendai virus nucleocapsids.Ambisense sendai viruses are inherently unstable but are useful to study viral RNA synthesis.Influenza virus polymerase basic protein 1 interacts with influenza virus polymerase basic protein 2 at multiple sites.The C proteins of human parainfluenza virus type 1 limit double-stranded RNA accumulation that would otherwise trigger activation of MDA5 and protein kinase RRole of a highly conserved NH(2)-terminal domain of the human parainfluenza virus type 3 RNA polymerase.Replication-coupled and host factor-mediated encapsidation of the influenza virus genome by viral nucleoprotein.An N-terminal domain of the Sendai paramyxovirus P protein acts as a chaperone for the NP protein during the nascent chain assembly step of genome replication.Independent structural domains in paramyxovirus polymerase protein.The Sendai paramyxovirus accessory C proteins inhibit viral genome amplification in a promoter-specific fashionAn amino-terminal domain of the Sendai virus nucleocapsid protein is required for template function in viral RNA synthesis.Characterization of the components and activity of Sonchus yellow net rhabdovirus polymerase.Evaluation of nucleocapsid and phosphoprotein p functionality as critical factors during the early phase of paramyxoviral infection.Role for the phosphoprotein P subunit of the paramyxovirus polymerase in limiting induction of host cell antiviral responsesNovel Strategy to Control Transgene Expression Mediated by a Sendai Virus-Based Vector Using a Nonstructural C Protein and Endogenous MicroRNAs.Interaction of vesicular stomatitis virus P and N proteins: identification of two overlapping domains at the N terminus of P that are involved in N0-P complex formation and encapsidation of viral genome RNA.Mumps Virus Nucleoprotein Enhances Phosphorylation of the Phosphoprotein by Polo-Like Kinase 1.Tacaribe virus Z protein interacts with the L polymerase protein to inhibit viral RNA synthesis.Mapping of a region of the paramyxovirus L protein required for the formation of a stable complex with the viral phosphoprotein P.The Tacaribe arenavirus small zinc finger protein is required for both mRNA synthesis and genome replication.Conformational maturation of measles virus nucleocapsid proteinThe hypervariable C-terminal tail of the Sendai paramyxovirus nucleocapsid protein is required for template function but not for RNA encapsidationInfluence of antigen insertion site and vector dose on immunogenicity and protective capacity in Sendai virus-based human parainfluenza virus type 3 vaccines.HSP90 Chaperoning in Addition to Phosphoprotein Required for Folding but Not for Supporting Enzymatic Activities of Measles and Nipah Virus L Polymerases.The L-VP35 and L-L interaction domains reside in the amino terminus of the Ebola virus L protein and are potential targets for antivirals.
P2860
Q24531423-06344442-3068-4774-ACD1-4D82EBC23FA7Q26851684-9BA0B139-A701-45E0-BFD2-9BD47ADF2E7BQ27325499-FA030F14-F820-41E0-A387-7B52108E0102Q27675573-80C2D022-795E-47D3-B9C9-1F0A5501225CQ27865305-289ED910-04F4-4AAE-BAD0-A44444494CE4Q30818098-69B398D8-56E8-4D64-81B6-46182713BB9AQ33604006-1BBFFB8D-950B-4063-9B3F-884AEB155736Q33653597-51C2E756-A2DD-4E18-9FD4-752C61A003CDQ33782318-3D882E44-55D2-4917-A86F-3DB7B064790EQ33782848-DBBB94BA-FF76-4E28-B4F6-13D2B2DFFCD7Q33785253-DB2508FF-D962-4A03-BC40-8E7E2C329AABQ33794492-E1AB628B-E0D8-4644-9BCD-2C61B9144CB5Q33820705-1DA8E32F-2334-4FBB-9581-CEBE7AF366F2Q33836020-BBEE57AE-50CB-4C25-815B-6229E0C8D0C2Q34025263-6620BD12-4F31-4C02-A9E3-6F1BD3FBB2F6Q34342086-53034C98-03C1-4BA0-8744-B12420D04086Q34364626-724F6795-AB1E-4228-9A83-C1E4CF8271B4Q34365261-4BC0D884-38F0-4FD5-9B10-03607F1F2A25Q34395842-23A7F138-3F99-4D84-B090-ACB41D4838D8Q34529862-50DC6DEB-FC90-4356-95F2-BD3D42805904Q35000831-0E2BB714-8ED0-4E62-8AE9-FF6FC01F3DB8Q35077609-7A145345-7E29-4381-BCF3-0F9E65504BA3Q35831672-1FBF537C-E6A2-4B16-AF12-681FE6551621Q35838944-48F66F99-3FF8-4258-A721-CED820EDD03AQ35865844-0FF0C8B3-3478-4E3D-8824-1DAEFB15EA79Q35876229-7C946F98-759B-4B10-9191-B85C00454D6FQ35879456-C9580F64-A627-4D98-A22C-DB4528BB61E7Q36081874-26195559-4485-4526-9B71-DDCA811D36B9Q36099330-2C451F88-4D83-400E-AC6D-97EF6A6703B1Q36169226-28AF9C90-1D0C-4D42-A473-8F4511B2E480Q36315226-9DA1109D-0FD5-4FD6-9267-77C8B6CFB4BCQ36481517-B1A6CD0F-1FE5-4F98-8603-1C52AE2B7C1DQ36525018-2C1A9F03-01C0-4E3D-8C17-624A424C02E6Q36624116-91A1B30B-8DE7-422D-B3ED-A8FECCC92B40Q36641126-9D717E33-C65C-4A6B-930C-2031A0307119Q36650153-52CE2D9E-1B77-40F5-999F-26A15BA0F6A6Q36650413-572ED263-D5C0-48F6-8DCE-F8884F76F782Q36827280-DA64992E-55A6-4963-87EF-A71C066394B0Q37093466-79B6378B-86A6-4FEE-A0F4-EF8ACF3A42C0Q37172020-1499AC81-8F82-40FC-AF2B-4CD313E7AB1C
P2860
Complexes of Sendai virus NP-P and P-L proteins are required for defective interfering particle genome replication in vitro.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@ast
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@en
type
label
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@ast
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@en
prefLabel
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@ast
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@en
P2093
P2860
P1433
P1476
Complexes of Sendai virus NP-P ...... e genome replication in vitro.
@en
P2093
Horikami SM
Kolakofsky D
P2860
P304
P407
P577
1992-08-01T00:00:00Z